chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105760678057606781TC14GENIChomozygous116604013
105760751257607513AG27GENIChomozygous116604017
105760788257607883TC22GENIChomozygous116604019
105760800957608010GC20GENIChomozygous116604021
105760847957608480GC21GENIChomozygous116604025
105760851557608516AG27GENIChomozygous116604027
105760926257609263CT30GENIChomozygous116604029
105760943157609432TC20GENIChomozygous116604031
105760993457609935GC10GENIChomozygous116604033
105761040857610409AG20GENIChomozygous117060318
105761083857610839AG15GENIChomozygous116604035
105761103957611040GA22GENIChomozygous116604039
105761244957612450CT32GENIChomozygous116785603
105761349657613497GA23GENIChomozygous116785605